HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1422457Generated: October 31, 2026
4,4'-Dibromobiphenyl → HCID 20650340, compound
https://huagongshe.com/reaction/1422457
Participants
| Role | Name | HCID | Charge |
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| Reactant | 4,4'-Dibromobiphenyl | HCID 7110 | — |
| Reactant | Benzenamine, 4-methyl-N-(4-methylphenyl)- | HCID 69293 | — |
| Reactant | Tris(1,1-dimethylethyl)phosphine | HCID 83681 | — |
| Reactant | Sodium t-butoxide | HCID 23676156 | — |
| Catalyst | Bis(dibenzylideneacetone)palladium | HCID 9811564 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 20650340 | HCID 20650340 | 3% |
Reaction Steps
A mixture of tris(dibenzylideneacetone)dipalladium (353 mg, 0.385 mmol), and tri-tert-butyl phosphine (3.11 g of a 10% solution in hexanes) was degassed in toluene (anhydrous, 50 mL) for 20 minutes. Di-p-tolylamine (3.00 g, 15.2 mmol), and 4,4′-dibromobiphenyl (4.80 g, 15.4 mmol) were added and the mixture was further degassed for 15 minutes. Sodium tert-butoxide (2.4 g, 25 mmol) was added, and mixture was further degassed for 10 minutes. The whole was heated overnight at 120° C. under argon. After cooling, the mixture was poured into DCM, and solids were filtered off. Filtrate was washed with water and brine. The organic layer was collected and dried over sodium sulfate, then loaded onto silica gel. A flash column (gradient of 2-20% ethyl acetate in hexanes) gave 190 mg of material (3% yield); confirmed pure by HNMR.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08927121B2 |
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| Source dataset | uspto-grants-2015_01 |
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| ORD ID | ord-55ba6f68ffa44527bcc5ebc89d24a7e2 |
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| Source note | uspto-grants-2015_01 |
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